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Deferred consent in a minimal-risk study involving critically ill subarachnoid hemorrhage patients

INTRODUCTION: Alterations from first-party and surrogate decision-maker consent can enhance the feasibility of research involving critically ill patients. OBJECTIVE: To describe the use of a deferred-consent model to enable participation of critically ill patients in a minimal-risk biomarker study....

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Main Authors: Topolovec-Vranic, Jane, Santos, Marlene, Baker, Andrew J, Smith, Orla M, Burns, Karen EA
Formato: Artigo
Idioma:Inglês
Publicado: Pulsus Group Inc 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4198231/
https://ncbi.nlm.nih.gov/pubmed/24914705
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